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Diclofenac sodium salt, Thermo Scientific Chemicals

Standard NSAID and cyclooxygenase (COX) inhibitor

$68.95 - $464.23

Chemical Identifiers

CAS 15307-79-6
Molecular Formula C14H10Cl2NNaO2
Molecular Weight (g/mol) 318.129
MDL Number MFCD00082251
InChI Key KPHWPUGNDIVLNH-UHFFFAOYSA-M
Synonym diclofenac sodium, sodium diclofenac, diclofenac sodium salt, voltaren, solaraze, anthraxiton, prophenatin, allvoran, batafil, delimon
PubChem CID 5018304
ChEBI CHEBI:4509
IUPAC Name sodium;2-[2-(2,6-dichloroanilino)phenyl]acetate
SMILES C1=CC=C(C(=C1)CC(=O)[O-])NC2=C(C=CC=C2Cl)Cl.[Na+]
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Products 3
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAJ6260906
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Thermo Scientific Chemicals
J6260906
5 g
Each for $68.95
 
AAJ6260914
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Thermo Scientific Chemicals
J6260914
25 g
Each for $152.44
 
AAJ6260922
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Thermo Scientific Chemicals
J6260922
100 g
Each for $464.23
 
Description

Description

Oxidation of diclofenac sodium produces the metabolite 4'-hydroxy diclofenac) which demonstrates specific inhibition of Cox-2. Inhibition of Cox by diclofenac and 4'-hydroxy diclofenac suppresses prostaglandin E2 synthesis, producing anti-inflammatory and analgesic effects. Diclofenac is also shown to stabilize the native tetrameric conformation of transthyretin (TTR) fibrils, preventing the formation of insoluble amyloidogenic TTR deposits. Diclofenac Sodium is a substrate of CYP2C9. It is also used as an inhibitor of Cox-1 and Cox-2.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Oxidation of diclofenac sodium produces the metabolite 4′-hydroxy diclofenac) which demonstrates specific inhibition of Cox-2. Inhibition of Cox by diclofenac and 4′-hydroxy diclofenac suppresses prostaglandin E2 synthesis, producing anti-inflammatory and analgesic effects. Diclofenac is also shown to stabilize the native tetrameric conformation of transthyretin (TTR) fibrils, preventing the formation of insoluble amyloidogenic TTR deposits. Diclofenac Sodium is a substrate of CYP2C9. It is also used as an inhibitor of Cox-1 and Cox-2.

Solubility
Soluble in water (50 mg/ml), PBS pH 7.2 (6 mg/ml), ethanol (∼35 mg/ml), DMF (∼35 mg/ml), DMSO (∼35 mg/ml), methanol (>24 mg/ml), and acetone (6 mg/ml).

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from strong oxidizing agents.
Specifications

Chemical Identifiers

15307-79-6
318.129
KPHWPUGNDIVLNH-UHFFFAOYSA-M
5018304
sodium;2-[2-(2,6-dichloroanilino)phenyl]acetate
C14H10Cl2NNaO2
MFCD00082251
diclofenac sodium, sodium diclofenac, diclofenac sodium salt, voltaren, solaraze, anthraxiton, prophenatin, allvoran, batafil, delimon
CHEBI:4509
C1=CC=C(C(=C1)CC(=O)[O-])NC2=C(C=CC=C2Cl)Cl.[Na+]

Specifications

15307-79-6
White
MFCD00082251
UN2811
diclofenac sodium, sodium diclofenac, diclofenac sodium salt, voltaren, solaraze, anthraxiton, prophenatin, allvoran, batafil, delimon
KPHWPUGNDIVLNH-UHFFFAOYSA-M
sodium;2-[2-(2,6-dichloroanilino)phenyl]acetate
5018304
318.14
Diclofenac sodium salt
283°C to 285°C
C14H10Cl2NNaO2
5 g
14,3081
Soluble in water to 50mg/ml.
C1=CC=C(C(=C1)CC(=O)[O-])NC2=C(C=CC=C2Cl)Cl.[Na+]
318.129
CHEBI:4509
Powder
Safety and Handling

Safety and Handling

GHS H Statement
H301-H361
Toxic if swallowed.
Suspected of damaging fertility or the unborn child.

P264b-P270-P301+P310-P330-P501c

H301

DOTInformation : Transport Hazard Class: 6.1; Packing Group: III; Proper Shipping Name: TOXIC SOLIDS, ORGANIC, N.O.S.

EINECSNumber : 239-346-4

RTECSNumber : AG6330000

TSCA : No

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only